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• W4242832223 abstract "Kationische Alkylyttrium-Halbsandwichkomplexe katalysieren die ortho-selektive Addition benzylischer C-H-Bindungen von Dialkylpyridinen an eine Reihe von Olefinen wie Ethylen, 1-Hexen, Styrole und 1,3-konjugierte Diene, bei der neue alkylierte und allylierte Pyridine erhalten werden (siehe Schema; Cp=C5Me5). Eine kationische Picolylyttrium-Halbsandwichspezies wie [CpY(2-CH2-6-CH3C5H3N)]+ wurde als entscheidende aktive Spezies bestätigt. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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• W4242832223 date "2013-03-19" @default.
• W4242832223 modified "2023-10-07" @default.
• W4242832223 title "Yttrium-Catalyzed Addition of Benzylic CH Bonds of Alkyl Pyridines to Olefins" @default.
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• W4242832223 doi "https://doi.org/10.1002/ange.201208867" @default.
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